Medical Device Recalls
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1 result found
510(K) Number: K111702 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AMICUS Exchange Kit; Product Usage: This kit is designed for use with the AMICUS separator for ... | 2 | 06/08/2013 | Fenwal Inc |
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